ABSTRACT
Abstract Synostosis is a generic term to indicate the union of two originally separated bones. At the elbow, humeroradial or longitudinal synostosis causes significant disability, which varies depending on hand function, elbow positioning, adjacent joints mobility and contralateral limb function. It is estimated that, to date, a little more than 150 patients have been described with this deformity, which is more common in subjects with deficient ulnar formation or affected by conditions such as Antley-Bixler and Hermann syndromes. The lack of the elbow joint, with the formation of a longer bone due to humerus-radius fusion, results in stiffness. As such, it is assumed that fractures in this topography are not uncommon. However, since synostosis is rare, this lesion was only described twice in the literature. We report two patients with a fracture of the single bone formed by a humeroradial synostosis and Bayne type-IV ulnar formation failure. Both patients were treated surgically with success. We emphasize the need for adequate treatment to not compromise the daily activities of patients who are adapted to their deformity, thus avoiding worsening the function of a previously affected limb.
Resumo Sinostose é um termo genérico utilizado para indicar a união de dois ossos originalmente separados. No cotovelo, a sinostose rádio-umeral ou longitudinal causa importante incapacidade, que varia a depender da função da mão, da posição do cotovelo, da mobilidade das articulações adjacentes e da função do membro contralateral. Estima-se que um pouco mais de 150 pacientes foram descritos até hoje com essa deformidade, sendo mais frequente em portadores de deficiência de formação ulnar ou podendo fazer parte de síndromes como de Antley-Bixler e de Hermann. Devidoàrigidezcausadapelaausênciadaarticulaçãodocotovelo,queresultana formação de um osso mais longo com a fusão do úmero no rádio, presume-se que fratura nessa topografia não seja incomum. No entanto, pela raridade dessa patologia, tal lesão apresenta apenas duas descrições prévias na literatura. Relatamos os casos de dois pacientes com fratura do osso único formado pela sinostose entre o úmero e o rádio portadores de falha de formação ulnar do tipo IV de Bayne. Ambos os pacientes foram tratados de forma cirúrgica e evoluíram bem. Salientamos a necessidade do tratamento adequado para não comprometer as atividades da vida de um paciente já adaptado à deformidade, evitando piorar a função de um membro já alterado.
Subject(s)
Humans , Male , Child , Middle Aged , Radio , Synostosis/surgery , Congenital Abnormalities , Ulna/abnormalitiesABSTRACT
BACKGROUND: Congenital radioulnar synostosis (CRUS) refers to an abnormal connection between the radius and ulna due to embryological failure of separation. Derotational osteotomy has been advocated for children with functional limitations, although historically this procedure has been associated with a 36% complication rate including compartment syndrome and loss of correction. METHODS: A retrospective evaluation of consecutive patients who underwent derotational osteotomy for CRUS at a single institution was performed. Children with functional limitations secondary to excessive pronation were indicated for surgery with a goal of correction to 10 to 20 degrees of pronation. All patients were treated with a standardized surgical technique including careful subperiosteal elevation, rotational osteotomy at the level of the synostosis, control of the osteotomy fragments, appropriate pinning techniques, and prophylactic forearm fasciotomies. Electronic medical records, preoperative radiographs, and postoperative radiographs were reviewed. RESULTS: Derotational osteotomy was performed in 31 forearms in 26 children (13 bilateral, 13 unilateral) with a mean age of 6.8 years (range, 3.0 to 18.8 y). The mean clinical follow-up was 46 months (range, 6 to 148 mo). The mean preoperative pronation deformity was 85 degrees (range, 60 to 100 degrees). The mean correction achieved was 77 degrees (range, 40 to 95 degrees), resulting in a mean final position of 8 degrees of pronation (range, 0 to 30 degrees). All patients successfully achieved union by 8 weeks postoperatively. There were no cases of compartment syndrome, vascular compromise, or loss of fixation. The overall complication rate was 12% (2 transient anterior interosseous nerve palsies, 1 transient radial nerve palsy, 1 symptomatic muscle herniation). Both transient anterior interosseous nerve palsies occurred in patients with rotational corrections exceeding 80 degrees. CONCLUSIONS: Derotational osteotomy can be safely and effectively performed in children with CRUS. Meticulous surgical technique, including control of the osteotomy, judicious pin fixation, and prophylactic fasiotomies, may diminish the risk of neurovascular compromise and loss of correction. Transient anterior interosseous nerve palsies occurred, and may be related to large rotational corrections.
Subject(s)
Forearm , Osteotomy , Radius/abnormalities , Synostosis , Ulna/abnormalities , Adolescent , Child , Child, Preschool , Female , Forearm/physiopathology , Forearm/surgery , Humans , Male , Osteotomy/adverse effects , Osteotomy/methods , Postoperative Period , Pronation/physiology , Radiography , Radius/diagnostic imaging , Radius/physiopathology , Radius/surgery , Retrospective Studies , Synostosis/diagnostic imaging , Synostosis/physiopathology , Synostosis/surgery , Treatment Outcome , Ulna/diagnostic imaging , Ulna/physiopathology , Ulna/surgeryABSTRACT
BACKGROUND: We report the case of a male, 15 year-old patient without any remarkable pathologic history, with double talocalcaneal and calcaneonavicular coalition in both feet. He underwent surgery of the left foot due to onset of refractory symptoms after conservative treatment. RESULTS: Both coalitions were resected and pedal muscle was interposed at the level of the calcaneonavicular joint as well as an endorthesis in the tarsal sinus. The patient became totally asymptomatic after surgery. CONCLUSIONS: Multiple bilateral tarsal coalitions, i.e., present in both feet, are very infrequent, except when they are associated with syndromic pictures or conditions such as fibular hemimelus, Alpert syndrome, Nievergelt-Pearlman syndrome, multiple synostosis or hereditary symphalangism. Treatment should be individualized based on the location of the synostosis.
Subject(s)
Subtalar Joint/surgery , Synostosis/surgery , Adolescent , Humans , Male , Orthopedic Procedures/methods , Treatment OutcomeSubject(s)
Infant, Newborn , Infant , Synostosis/surgery , Humerus/abnormalities , Radius/abnormalities , Hand Deformities, Congenital , Elbow Joint/abnormalities , Elbow Joint/pathology , Elbow Joint/surgery , Musculoskeletal Abnormalities , Heart Defects, Congenital , Upper Extremity/embryology , Treatment OutcomeSubject(s)
Infant, Newborn , Infant , Synostosis/surgery , Humerus/abnormalities , Radius/abnormalities , Hand Deformities, Congenital , Elbow Joint/abnormalities , Elbow Joint/pathology , Elbow Joint/surgery , Musculoskeletal Abnormalities , Heart Defects, Congenital , Upper Extremity/embryology , Treatment OutcomeSubject(s)
Infant, Newborn , Infant , Musculoskeletal Abnormalities , Elbow Joint/abnormalities , Elbow Joint/surgery , Elbow Joint/pathology , Hand Deformities, Congenital , Humerus/abnormalities , Radius/abnormalities , Synostosis/surgery , Heart Defects, Congenital , Upper Extremity/embryology , Treatment OutcomeSubject(s)
Humans , Female , Middle Aged , Surgery, Oral , Molar , Radiography, Panoramic , Synostosis/surgeryABSTRACT
The purpose of this paper is to present an alternative method of achieving a synostosis between tibia and fibula in trans-tibial amputations by means of a fibular segment in place of tibial osteoperiosteal flaps as described by Ertl, in 1949. From May 1997 through to February 2003, 15 patients were submitted to the proposed procedure. As a result, all patients produced a solid synostosis between tibia and fibula and were rehabilitated with the use of prostheses. The capacity of these patients for distal weight-bearing on the stump was remarkable when compared to patients submitted to the conventional trans-tibial amputation technique.
Subject(s)
Amputation, Surgical/methods , Osseointegration , Tibia/surgery , Adult , Aged , Amputation, Surgical/rehabilitation , Amputation Stumps , Bone Transplantation/methods , Female , Femur/surgery , Fibula/transplantation , Humans , Male , Middle Aged , Muscle, Skeletal/surgery , Surgical Flaps , Synostosis/surgery , Treatment OutcomeSubject(s)
Humans , Infant , Male , Child, Preschool , INFORME DE CASO , Synostosis/surgery , Craniotomy/methodsABSTRACT
Os casos de sinostose congênita radioulnal proximal registrados no Serviço de Ortopedia e Traumatologia do Hospital Municipal Jesus (RJ) nos últimos 14 anos foram revistos e os resultados do tratamento analisados. Dez casos foram acompanhados entre 1975 e 1988, num total de comprometimentos de treze antebraços. Em sete casos a deformidade era unilateral e em três bilateral